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首页> 外文期刊>Tetrahedron >Stereoselective dimerization of 3-arylisoxazoles to cage-shaped bis-β-lactams syn 2,6-diaryl-3,7-diazatricyclo[4.2.0.02,5]octan-4,8-diones induced by hindered lithium amides
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Stereoselective dimerization of 3-arylisoxazoles to cage-shaped bis-β-lactams syn 2,6-diaryl-3,7-diazatricyclo[4.2.0.02,5]octan-4,8-diones induced by hindered lithium amides

机译:受阻锂酰胺诱导的3-芳基异恶唑立体选择性二聚为笼形双β-内酰胺合成2,6-二芳基-3,7-二氮三环[4.2.0.02,5]辛-4,8-​​二酮

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摘要

3-Arylisoxazoles react with hindered lithium amides giving syn 2,6-diaryl-3,7-diazatricyclo[4.2.0.02,5]octan-4,8-diones in good to fair yields. Stereochemistry of the so-obtained cage-shaped bis-β-lactams was assigned by X-ray diffraction analysis. Concerning the mechanism of formation of such hitherto unknown molecules, dimerization of an azetinone anion intermediate stereoselectively induced by Li+ chelation is suggested.
机译:3-Arylisoxazoles与受阻的锂酰胺反应生成顺式2,6-二芳基-3,7-二氮杂三环[4.2.0.02,5] octan-4,8-​​二酮,收率良好。通过X射线衍射分析确定所获得的笼状双β-内酰胺的立体化学。关于这种迄今未知分子的形成机理,提出了由Li +螯合立体诱导的氮杂环丁烷酮阴离子中间体的二聚化。

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